Journal
JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
Volume 28, Issue 4, Pages 272-280Publisher
SAGE PUBLICATIONS INC
DOI: 10.1177/0891988715598229
Keywords
Alzheimer disease; family caregivers; depressive symptoms; distress; spousal caregivers
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Funding
- Yrjo Jahnsson Foundation
- Finnish Brain Research and Rehabilitation Foundation Center Neuron
- Social Insurance Institute of Finland (Kela)
- Novartis Pharma AG
- Kuopio University Hospital (EVO/VTR) [5220/5772728]
- Finnish Nurses Association
- Foundation of Municipal Development in Finland
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Objective: To explore family caregiver (FC) long-term psychological distress after Alzheimer disease (AD) diagnosis in a family member. Methods: FC (n = 236) and patients with AD were prospectively followed up to 36 months after AD diagnosis. FC psychological distress was evaluated using the General Health Questionnaire (GHQ). Furthermore, caregiver depressive symptoms and sense of coherence, along with AD patient measurements, were measured at baseline and annually. Generalized estimating equation models were applied to study associations of these baseline factors to caregiver GHQ. Results: After 36 months of follow-up, spousal caregivers (SCs) GHQ was significantly higher (P < .001) than in the nonspousal caregivers (NSCs). The difference in GHQ scores was associated by depressive symptoms (P < .001) at baseline, and the depressed SCs have more severe distress than NSCs over the observation period. Conclusion: During longitudinal caregiving, spousal and depressed caregivers of patients with AD report higher and increasing psychological stress than nonspousal and nondepressed caregivers. Spousal relationship, caregivers' depressive symptoms, and the severity of patients' neuropsychological symptoms at the time of AD diagnosis predict the trajectory of psychological distress. The current study highlights the need for evaluating AD caregiver mental health and level of coping.
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